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Orchestra BioMed Announces Further Details on In-Person R&D Day in New York Featuring Key Opinion Leaders to Discuss AVIM Therapy Program in Hypertensive Pacemaker Patients on June 11, 2024

Orchestra BioMed Announces Further Details on In-Person R&D Day in New York Featuring Key Opinion Leaders to Discuss AVIM Therapy Program in Hypertensive Pacemaker Patients on June 11, 2024

Orchestra BioMed發佈有關2024年6月11日在紐約舉行的面對面研發日的進一步細節,重點是討論高血壓心臟起搏器患者的AVIM治療方案的專家意見。
GlobeNewswire ·  06/04 08:00

NEW HOPE, Pa., June 04, 2024 (GLOBE NEWSWIRE) -- Orchestra BioMed Holdings, Inc. (Nasdaq: OBIO, "Orchestra BioMed" or the "Company"), a biomedical company accelerating high-impact technologies to patients through risk-reward sharing partnerships, today announced further details on its in-person R&D day at the Lotte New York Palace Hotel on Tuesday, June 11, 2024, at 10:00 AM ET. To register, click here.

2024年6月4日,賓夕法尼亞州紐霍普(NEW HOPE),環球新聞社(GLOBE NEWSWIRE)——生物醫學公司Orchestra BioMed Holdings, Inc.(納斯達克股票代碼:OBIO,“Orchestra BioMed”或“公司”)通過風險共享合作伙伴加速將高影響力技術提供給患者,並宣佈了有關其親自出席的研發日在2024年6月11日星期二上午10:00美國東部時間於紐約麗笙酒店(Lotte New York Palace Hotel)的進一步細節。請登錄註冊。點擊這裏.

The R&D day will feature in-depth presentations focused on the Company's lead program, atrioventricular interval modulation (AVIM) therapy, including:

研發日將涵蓋公司的主導項目房間傳導耦合率(AVIM)治療方案。其內容包括:

  • The high unmet need for treatment of uncontrolled hypertension in pacemaker-indicated patients and other older high-risk patients
  • The AVIM therapy mechanism of action and supporting clinical and non-clinical mechanistic data
  • The robust existing body of clinical evidence from the MODERATO I and II studies
  • Design of and rationale for the BACKBEAT global pivotal study
  • 起搏器指徵患者等年長的高危患者對難以控制的高血壓治療的高不滿意需求
  • AVIM治療機制及其支持的臨床和非臨床機制數據
  • 現有的臨床證據——MODERATO I和II研究的實力
  • 全球關鍵研究——BACKBEAT的設計及其基本原理

In addition to Orchestra BioMed management presentations, the event will include esteemed key opinion leading physicians:

除了Orchestra BioMed的管理演示之外,該活動還將邀請傑出的主要意見領袖醫生:

David Kandzari, M.D., FACC, FSCAI, Chief of the Piedmont Heart Institute and Cardiovascular Service Line; Director, Interventional Cardiology of the Piedmont Heart Institute; Chief Scientific Officer for Piedmont Healthcare in Atlanta, Georgia; and co-principal investigator on the BACKBEAT global pivotal study

David Kandzari博士,FACC,FSCAI,皮德蒙特心臟研究所和心血管服務部的首席醫師; 作爲BACKBEAT全球關鍵研究的聯合首席調查員,是佐治亞州亞特蘭大皮德蒙特保健的首席科學官

  • Dr. Kandzari specializes in cardiovascular disease, peripheral arterial disease and interventional cardiology. Board certified by the American Board of Internal Medicine and its subspecialty Board of Cardiovascular Disease and Board of Interventional Cardiology, Dr. Kandzari has held national and international leadership roles in clinical trials in cardiovascular disease and has participated in national and international program committees in cardiology. He has authored and coauthored more than 400 studies, book chapters and scientific reviews, and has delivered more than 800 lectures, both nationally and internationally, on a variety of issues related to both interventional and general cardiology. Dr. Kandzari has been consecutively voted as one of Atlanta's Top Doctors by Atlanta Magazine from 2011 to 2024 and is peer-nominated in the top 1% of cardiologists by U.S News and World Report.
  • Kandzari博士專門治療心血管疾病、周圍動脈疾病和介入性心臟病學。Kandzari博士通過美國內科醫師委員會及其心血管疾病和介入性心臟病的子專業委員會以及介入性心臟病的委員組織國家和國際臨床試驗的領導角色。他已著作和合著了超過400篇研究、書籍章節和科學評論,並在與介入性和一般心血管相關的各種問題上在全球超過800場報告中發表。Kandzari博士連續自2011年至2024年被亞特蘭大雜誌評選爲亞特蘭大頂級醫生,並被美國新聞和世界報道同行提名爲心臟病學家中最佳的1%。

Vivek Reddy, M.D., Director of Cardiac Arrhythmia Services for The Mount Sinai Hospital and the Mount Sinai Health System; Leona M. and Harry B. Helmsley Charitable Trust Professor of Medicine in Cardiac Electrophysiology at Icahn School of Medicine at Mount Sinai; and Clinical Steering Committee Advisor for the BACKBEAT global pivotal study

Vivek Reddy博士,是賽樂瑞姆斯有節律專業服務的主任,是耶路撒冷山西奈醫學院的心臟電生理學中的Leona M.和Harry B. Helmsley慈善信託教授,並是BACKBEAT的臨床指導委員會顧問

  • Dr. Reddy is one of the nation's premier cardiac electrophysiologists, leading a team of physician-scientists who are developing and testing advanced therapies for cardiac arrhythmias – including atrial fibrillation and ventricular tachycardias, the most common cause of sudden cardiac death. Dr. Reddy's pioneering clinical research is changing the way cardiac patients are treated and cured. Under his leadership, Mount Sinai is the lead site on several multinational clinical trials exploring new arrhythmia procedures and technologies. In 2014, Dr. Reddy implanted the world's first miniature leadless pacemaker in a patient's heart in the United States at The Mount Sinai Hospital.
  • Reddy博士是美國首屈一指的心臟電生理學家之一,領導着一個由醫學專家組成的團隊,爲心律失常——包括房顫和室性心動過速,這是突然心臟死亡的最常見原因進行先進的治療和測試。Reddy博士的開創性的臨床研究正在改變心臟患者的治療和治癒方式。在他的領導下,Mount Sinai是探索新的心律失常程序和技術的國際多中心臨床試驗的首席參與網站。在2014年,Reddy博士在美國的The Mount Sinai醫院爲患者的心臟植入了世界上第一枚微型無引線起搏器。

A live question and answer session will follow formal presentations.

正式演示後將進行現場問答環節。

About Orchestra BioMed

關於Orchestra BioMed

Orchestra BioMed (Nasdaq: OBIO) is a biomedical innovation company accelerating high-impact technologies to patients through risk-reward sharing partnerships with leading medical device companies. Orchestra BioMed's partnership-enabled business model focuses on forging strategic collaborations with leading medical device companies to drive successful global commercialization of products it develops. Orchestra BioMed's lead product candidate is atrioventricular interval modulation (AVIM) therapy (also known as BackBeat Cardiac Neuromodulation Therapy (CNT)) for the treatment of hypertension, a significant risk factor for death worldwide. Orchestra BioMed is also developing Virtue Sirolimus AngioInfusion Balloon (SAB) for the treatment of atherosclerotic artery disease, the leading cause of mortality worldwide. Orchestra BioMed has a strategic collaboration with Medtronic, one of the largest medical device companies in the world, for the development and commercialization of AVIM therapy for the treatment of hypertension in pacemaker-indicated patients, and a strategic partnership with Terumo, a global leader in medical technology, for the development and commercialization of Virtue SAB for the treatment of artery disease. For further information about Orchestra BioMed, please visit , and follow us on LinkedIn.

Orchestra BioMed(納斯達克:OBIO)是一家生物醫學創新公司,通過風險共享合作伙伴與領先的醫療器械公司合作,將高影響力技術加速應用於患者身上。Orchestra BioMed的合作伙伴關係業務模式專注於與領先的醫療器械公司建立戰略合作關係,以推動其所開發產品的成功全球商業化。Orchestra BioMed的主要產品候選是房室間期調製(AVIM)療法(也稱爲BackBeat心臟神經調節療法(CNT))用於高血壓的治療,這是導致全球死亡的重要風險因素。Orchestra BioMed還正在開發Virtue 司羅莫斯血管輸注球囊(SAB),用於治療動脈粥樣硬化性動脈疾病,這是全球死亡的主要原因。Orchestra BioMed與Medtronic達成了戰略合作關係,後者是全球最大的醫療器械公司之一,目的是開發和商業化針對起搏器指徵患者的血壓高療法,以及與Terumo達成戰略伙伴關係,後者是全球醫療技術的領導者,目的是開發和商業化Virtue SAB以治療動脈疾病。更多有關Orchestra BioMed的信息,請訪問網站,並在領英上關注我們。

References to Websites and Social Media Platforms

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References to information included on, or accessible through, websites and social media platforms do not constitute incorporation by reference of the information contained at or available through such websites or social media platforms, and you should not consider such information to be part of this press release.

關於高血壓及起搏器患者高血壓風險

About Hypertension and the Risk of High Blood Pressure in the Pacemaker Population

高血壓(“ HTN”)的特徵是血壓升高,這增加了推動血液通過血管的壓力,要求心臟更加努力地工作和消耗更多的氧氣。高血壓加快動脈粥樣硬化的進程,並導致諸如心臟病發作、心力衰竭、腎臟疾病和其他內臟器官損傷等主要心臟事件的風險增加。高血壓是全球主要的死亡風險因素,影響全球約128億成年人。在美國,估計有1.22億成年人,約佔所有成年人的47%。雖然許多患者沒有注意到自己的高血壓,但隨着收縮壓每升高10毫米汞柱,心血管風險加倍,而收縮壓增加20毫米汞柱,死亡率也會倍增。

Hypertension ("HTN") is characterized by elevated blood pressure, which increases the force of blood pushing against blood vessels, requiring the heart to work harder and consume more oxygen. HTN accelerates the progression of atherosclerosis and leads to increased risk of major cardiac events like heart attack, heart failure, kidney disease and other end organ damage. HTN is the leading global risk factor for death, affecting an estimated 1.28 billion adults worldwide. In the United States, 122 million adults, or approximately 47% of all adults, are estimated to have HTN. While many patients do not notice high blood pressure, cardiovascular risk doubles for every 10-mmHg increase in systolic blood pressure and the mortality rate doubles with an increase of 20 mmHg in systolic blood pressure.1

據估計,每年有超過110萬人植入心臟起搏器的全球約70%以上的患者被診斷爲患有高血壓。根據美國心臟病學會/美國心臟協會的最新指南,我們估計美國80%左右的起搏器適應症患者患有高血壓。起搏器患者往往年齡較大,更可能患有共病症,如動脈粥樣硬化、高脂血症、糖尿病和慢性腎臟疾病,並且由於共病症高發和難以有效治療,包括單純收縮期高血壓在內的患病率也相對較高。1

It is estimated that more than 70% of the approximately 1.1 million people globally who are implanted with cardiac pacemakers each year are also diagnosed with HTN. Based on updated American College of Cardiology/American Heart Association guidelines, we estimate that an even higher percentage (approximately 80%) of U.S. patients who are indicated for a pacemaker implant have HTN. Pacemaker patients tend to be elderly and are more likely to suffer from co-morbidities, such as atherosclerosis, hyperlipidemia, diabetes mellitus and chronic kidney disease, and harder to treat effectively with medical therapy for many reasons, including co-morbidities and a high prevalence of isolated systolic HTN.

關於AVIM療法(BackBeat CNT)

About AVIM Therapy (BackBeat CNT)

開展高血壓治療的創新技術是Orchestra BioMed的優先事項。AVIM治療是一種非藥物侵入性治療高血壓的技術,它是通過在房室間期內應用心臟神經控制來減少心臟負擔,並已得到臨床(MODERATO I和II試驗)和非臨床研究的廣泛支持。該技術嵌入式於現有起搏器系統,或使用單獨的診斷或治療外部電極,並已被證明是在患者群中易於操作的和重複的。AVIM治療的一種參考形式——BackBeat心臟神經調節療法(CNT)——針對有助於起搏器指標的患者的需求,已進行前瞻性的多中心全球試驗,名爲BACKBEAT全球關鍵研究。接受此治療的第一個患者已在歐盟獲批。

AVIM therapy, also known as BackBeat CNT, is an investigational therapy compatible with standard dual-chamber pacemakers designed to substantially and persistently lower blood pressure. It has been evaluated in pilot studies in patients with hypertension who are also indicated for a pacemaker. MODERATO II, a double-blind, randomized, pilot study, showed that patients treated with AVIM therapy experienced net reductions of 8.1 mmHg in 24-hour ambulatory systolic blood pressure (aSBP) and 12.3 mmHg in office systolic blood pressure (oSBP) at six months when compared to control patients. The IDE approved BACKBEAT (BradycArdia paCemaKer with atrioventricular interval modulation for Blood prEssure treAtmenT) global pivotal study will further evaluate the safety and efficacy of AVIM therapy in lowering blood pressure in a similar target population of patients who have been indicated for, and recently implanted with, a dual-chamber cardiac pacemaker.

AVIM療法,又稱BackBeat CNT,是一種符合標準雙腔起搏器的新型療法,可以顯著和持久地降低血壓。它已經在高血壓患者中進行了 pilot 研究,這些患者同時也適用於自動體外心臟起搏器。MODERATO II 是一項雙盲、隨機、pilot 研究,該研究表明,與對照組患者相比,接受 AVIM 療法治療的患者在6個月時24小時動態血壓監測收縮壓(aSBP)和辦公室測量收縮壓(oSBP)的淨降壓量分別爲8.1毫米汞柱和12.3毫米汞柱。FDA已批准BACKBEAT研究(BradycArdia paCemaKer with atrioventricular interval modulation for Blood prEssure treAtmenT),該全球關鍵研究將進一步評估AVIM療法在類似的雙腔心臟起搏器患者群中降低血壓的安全性和療效。

References:

參考文獻:

1. Benjamin EJ, Blaha MJ, Chiuve SE, et al., Heart Disease and Stroke Statistics – 2017 Update: A Report from the American Heart Association. Circulation. 2017; 135: e146.

1. Benjamin EJ、Blaha MJ、Chiuve SE等。《心臟病和中風綜合統計數據-2017年更新:來自美國心臟協會的報告》。《循環》。2017; 135:e146。

Investor Contact:
Bob Yedid
LifeSci Advisors
(516) 428-8577
Bob@lifesciadvisors.com

投資者聯繫人:
Bob Yedid
LifeSci Advisors
(516) 428-8577
Bob@lifesciadvisors.com

Media Contact:
Kelsey Kirk-Ellis
Orchestra BioMed
(484) 682-4892
Kkirkellis@orchestrabiomed.com

媒體聯繫人:
Kelsey Kirk-Ellis
Orchestra BioMed
(484) 682-4892
Kkirkellis@orchestrabiomed.com


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